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M B Poh-Fitzpatrick

Showing results (71-80 of 83) with videos related to

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Archives of Dermatology|April 1, 1985
Quinidine photosensitivityR B Armstrong, E E Leach, G Whitman, et al.
The New England Journal of Medicine|August 10, 1978
Porphyria cutanea tarda in two patients treated with hemodialysis for chronic renal failureM B Poh-Fitzpatrick, N Bellet, V A DeLeo, et al.
The American Journal of Medicine|August 1, 1979
Porphyria cutanea tarda. Clinical features and laboratory findings in 40 patientsM E Grossman, D R Bickers, M B Poh-Fitzpatrick, et al.
Archives of Dermatology|September 1, 1992
Congenital erythropoietic porphyria. A mild variant with low uroporphyrin I levels due to a missense mutation (A66V) encoding residual uroporphyrinogen III synthase activityC A Warner, M B Poh-Fitzpatrick, E F Zaider, et al.
Hepatology (Baltimore, Md.)|December 1, 1989
Interaction of hemopexin, albumin and liver fatty acid-binding protein with protoporphyrinE Knobler, M B Poh-Fitzpatrick, D Kravetz, et al.
The Journal of Investigative Dermatology|July 27, 1999
Haplotype analysis of families with erythropoietic protoporphyria and novel mutations of the ferrochelatase geneX Wang, L Yang, L Kurtz, et al.
Pediatric Dermatology|August 1, 1988
Photodermatosis in infants and childrenM B Poh-Fitzpatrick, C A Ramsay, W Frain-Bell, et al.
The New England Journal of Medicine|March 12, 1987
Hepatoerythropoietic porphyria: clinical, biochemical, and enzymatic studies in a three-generation family lineageA C Toback, S Sassa, M B Poh-Fitzpatrick, et al.
Archives of Dermatology|August 1, 1978
Hydroa vacciniformeD R Bickers, L K Demar, V DeLeo, et al.
Gastroenterology|September 1, 1990
Cutaneous photosensitivity and coproporphyrin abnormalities in the Alagille syndromeM B Poh-Fitzpatrick, E Zaider, C Sciales, et al.
Pageof 9

Showing results (71-80 of 83) with videos related to

Sort By:
Pageof 9
Archives of Dermatology|April 1, 1985
Quinidine photosensitivityR B Armstrong, E E Leach, G Whitman, et al.
The New England Journal of Medicine|August 10, 1978
Porphyria cutanea tarda in two patients treated with hemodialysis for chronic renal failureM B Poh-Fitzpatrick, N Bellet, V A DeLeo, et al.
The American Journal of Medicine|August 1, 1979
Porphyria cutanea tarda. Clinical features and laboratory findings in 40 patientsM E Grossman, D R Bickers, M B Poh-Fitzpatrick, et al.
Archives of Dermatology|September 1, 1992
Congenital erythropoietic porphyria. A mild variant with low uroporphyrin I levels due to a missense mutation (A66V) encoding residual uroporphyrinogen III synthase activityC A Warner, M B Poh-Fitzpatrick, E F Zaider, et al.
Hepatology (Baltimore, Md.)|December 1, 1989
Interaction of hemopexin, albumin and liver fatty acid-binding protein with protoporphyrinE Knobler, M B Poh-Fitzpatrick, D Kravetz, et al.
The Journal of Investigative Dermatology|July 27, 1999
Haplotype analysis of families with erythropoietic protoporphyria and novel mutations of the ferrochelatase geneX Wang, L Yang, L Kurtz, et al.
Pediatric Dermatology|August 1, 1988
Photodermatosis in infants and childrenM B Poh-Fitzpatrick, C A Ramsay, W Frain-Bell, et al.
The New England Journal of Medicine|March 12, 1987
Hepatoerythropoietic porphyria: clinical, biochemical, and enzymatic studies in a three-generation family lineageA C Toback, S Sassa, M B Poh-Fitzpatrick, et al.
Archives of Dermatology|August 1, 1978
Hydroa vacciniformeD R Bickers, L K Demar, V DeLeo, et al.
Gastroenterology|September 1, 1990
Cutaneous photosensitivity and coproporphyrin abnormalities in the Alagille syndromeM B Poh-Fitzpatrick, E Zaider, C Sciales, et al.
Pageof 9